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The clinical laboratory improvement amendments (clia) of 1988 are united states federal regulatory standards that apply to all clinical laboratory testing performed on humans in the united states, except clinical trials and basic research. A similar guideline for clinical trials of medical devices is the international standard iso 14155, which is valid in the european union as a harmonized standard Clsi promotes the development and use of voluntary laboratory consensus standards and guidelines within the health care community.
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Medical billing, a payment process in the united states healthcare system, is the process of reviewing a patient's medical records and using information about their diagnoses and procedures to determine which services are billable and to whom they are billed. Iso 15189 medical laboratories — requirements for quality and competence is an international standard that specifies the quality management system requirements particular to medical laboratories. The cpt code set describes medical, surgical, and diagnostic services and is designed to communicate uniform information about medical services and procedures among physicians, coders, patients, accreditation organizations, and payers for administrative, financial, and analytical purposes.
The clinical data interchange standards consortium (cdisc) is a standards developing organization (sdo) dealing with medical research data linked with healthcare,made to enable information system interoperability and to improve medical research and related areas of healthcare.
Good clinical laboratory practice (gclp) is a gxp guideline for laboratory samples from clinical studies
